All variants

Continuously updated · newest added Sep 12, 2026

7,519 variants MyGeneLog™ checks for — each with its own plain-language page and cited source. New findings are collected from the public GWAS Catalog every twenty minutes.

Standard on its own

Urinary metabolites

AGXT · rs6748734

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Standard on its own

Urinary metabolites

SLC6A13 · rs11062102

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Standard on its own

Urinary metabolites

SLC6A19 · rs11133665

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Sensitive

Inflammatory bowel disease

PMVK · rs3766920

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Sensitive

Incident myocardial infarction

QKI · rs6941513

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Standard on its own

Caffeine metabolism (plasma 1,7-dimethylxanthine (paraxanthine) to 1,3,7-trimethylxanthine (caffeine) ratio)

AHR · rs2892838

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Standard

Caffeine metabolism (plasma 1,7-dimethylxanthine (paraxanthine) to 1,3,7-trimethylxanthine (caffeine) ratio)

CYP2A6 · rs184589612

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Standard

Caffeine metabolism (plasma 1,7-dimethylxanthine (paraxanthine) to 1,3,7-trimethylxanthine (caffeine) ratio)

CYP2A6 · rs66500423

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Standard on its own

Caffeine metabolism (plasma 1,7-dimethylxanthine (paraxanthine) to 1,3,7-trimethylxanthine (caffeine) ratio)

ARID3B · rs2470893

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Standard on its own

Caffeine metabolism (plasma 1,3,7-trimethylxanthine (caffeine) level)

AHR · rs10275488

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Standard on its own

Caffeine metabolism (plasma 1,3,7-trimethylxanthine (caffeine) level)

ARID3B · rs35107470

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Standard on its own

Caffeine metabolism (plasma 1,3,7-trimethylxanthine (caffeine) level)

ARID3B · rs12909047

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Standard

Gut microbiota (bacterial taxa)

NCAM1 · rs17115310

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Standard on its own

Modified Stumvoll Insulin Sensitivity Index (model adjusted for BMI)

IRS1 · rs7578326

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Standard on its own

Modified Stumvoll Insulin Sensitivity Index (model adjusted for BMI)

NYAP2 · rs13422522

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Standard

Gut microbiota (functional units)

HIVEP3 · rs12563071

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Standard

Gut microbiota (functional units)

SLIT3 · rs2163761

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Standard

Heart rate

CPNE8 · rs826838

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Standard

Heart rate

CD46 · rs11118555

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Standard

Gut microbiota (functional units)

SULT1C2 · rs17770672

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Questions about variants on this site

What is a "variant" page on this site?

One specific position in the genome (an rsID), explained in plain language with what published research has found it linked to, and how strong that link actually is.

Where does new variant data come from?

The public GWAS Catalog, checked every twenty minutes, plus variants added manually after research review. Every one passes the same quality gate before publishing.

Does being listed here mean a variant causes a condition?

No. Listing reflects an association from published research, not a diagnosis or a cause. Most common variants shift probability modestly rather than determining an outcome.

Can I search this list by gene or rsID?

Yes — the search box above matches gene symbols and rsIDs as well as trait names.